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rs11777116

From SNPedia

Orientationplus
Stabilizedplus
Make rs11777116(C;C)
Make rs11777116(C;T)
Make rs11777116(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position24186788
is asnp
is mentioned by
dbSNPrs11777116
ebirs11777116
HLIrs11777116
Exacrs11777116
Varsomers11777116
Maprs11777116
PheGenIrs11777116
hapmaprs11777116
1000 genomesrs11777116
hgdprs11777116
ensemblrs11777116
gopubmedrs11777116
geneviewrs11777116
scholarrs11777116
googlers11777116
pharmgkbrs11777116
gwascentralrs11777116
openSNPrs11777116
23andMers11777116
23andMe allrs11777116
SNP Nexus

SNPshotrs11777116
SNPdbers11777116
MSV3drs11777116
GWAS Ctlgrs11777116
GMAF0.09045
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine - clinic-based
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele T
P-val 6E-8
Odds Ratio 1.27 [1.17-1.39]